α-hemolysin variants with altered characteristics

ABSTRACT

Described herein are variants of alpha-hemolysin having at least one mutation selected from T12R, T12K, N17R, N17K or combinations of T12 and N17 mutations. The variants in some embodiments may further comprise H144A. The α-hemolysin variants have a decreased time to thread.

CROSS-REFERENCE TO RELATED APPLICATIONS

The present application claims priority to U.S. Provisional PatentApplication Ser. No. 62/073,936, entitled “alpha-Hemolysin Variants”,filed 31 Oct. 2014.

SEQUENCE LISTING

A sequence listing comprising SEQ ID NOS: 1-8 is attached hereto. Eachsequence provided in the sequence listing is incorporated herein byreference, in its entirety, for all purposes. Said ASCII copy, createdon Oct. 26, 2015, is named 20-04338.P519US1_SL.txt and is 20,325 bytesin size.

TECHNICAL FIELD

Disclosed are compositions and methods relating to Staphylococcalaureaus alpha-hemolysin variants. The alpha-hemolysin (α-HL) variantsare useful, for example, as a nanopore in a device for determiningpolymer sequence information. The nanopores, methods and systemsdescribed herein provide quantitative detection of single strand nucleicacids, such as DNA, RNA, etc., employing nanopore-based single-moleculetechnology with improved characteristics.

BACKGROUND

Hemolysins are members of a family of protein toxins that are producedby a wide variety of organisms. Some hemolysins, for example alphahemolysins, can disrupt the integrity of a cell membrane (e.g., a hostcell membrane) by forming a pore or channel in the membrane. Pores orchannels that are formed in a membrane by pore forming proteins can beused to transport certain polymers (e.g., polypeptides orpolynucleotides) from one side of a membrane to the other.

Alpha-hemolysin (α-HL, a-HL or alpha-HL) is a self-assembling toxinwhich forms an aqueous channel in the membrane of a host cell. Alpha-HLhas become a principal component for the nanopore sequencing community.It has many advantageous properties including high stability, selfassembly and a pore diameter which is wide enough to accommodate singlestranded DNA but not double stranded DNA (Kasianowicz et al., 1996).

Previous work on DNA detection in the a-HL pore has focused on analyzingthe ionic current signature as DNA translocates through the pore(Kasianowicz et al., 1996, Akeson et al., 1999, Meller et al., 2001), avery difficult task given the translocation rate (˜1 nt/μs at 100 mV)and the inherent noise in the ionic current signal. Higher specificityhas been achieved in nanopore-based sensors by incorporation of probemolecules permanently tethered to the interior of the pore (Howorka etal., 2001a and Howorka et al., 2001b; Movileanu et al., 2000).

The wild-type a-HL results in significant number of deletion errors,i.e. bases are not measured. Therefore, α-HL nanopores with improvedproperties are desired.

BRIEF SUMMARY OF THE INVENTION

The invention features a mutant staphylcoccal alpha hemolysin (αHL)polypeptide containing an amino acid variation that enhances the time tothread, e.g., decreases the time to capture of the molecule of interest.

The presently disclosed variants reduce the time thread of the moleculeof interest, e.g., various tagged nucleotides or a nucleotide to besequenced.

Disclosed herein are α-hemolysin (αHL) variants. The α-hemolysin (αHL)variants are derived from a parental α-HL polypeptide or a sequencehaving at least 80%, 90%, 95%, 98%, or more sequence identity to SEQ IDNO: 8, and comprises a substitution at a position corresponding toposition 12 or 17 of SEQ ID NO:3 (mature a-HL). In some embodiments, thevariant further comprises H144A. In some embodiments, the substitutioncomprises one or more positive charges. In some embodiments, the variantcomprises a substitution at a position corresponding to one or more ofresidues T12 and/or N17. In some embodiments, the variant comprises asubstitution selected from T12K, T12R, N17K, N17R and combinationsthereof. In some embodiments, the variant has an altered time to thread(TTT) relative to the parent α-hemolysin. In some embodiments, the TTTis decreased. In some embodiments, the variant comprises a substitutionat a position corresponding to a residue selected from the groupconsisting of T12R or K, and/or N17R or K in α-hemolysin (αHL) fromStaphylococcus aureus (SEQ ID NO: 1). In some embodiments, thesubstitution is T12K. In some embodiments, the substitution is T12R. Insome embodiments, the substitution is N17K. In some embodiments, thesubstitution is N17R. In some embodiments, the variant a-HL having analtered characteristic as compared to a parental α-hemolysin (e.g.,AAA26598) comprises H144A and at least one additional mutation selectedfrom

-   -   a. T12K/R;    -   b. N17K/R;        or combinations thereof.

In all embodiments, the alpha-hemolysin has a sequence having at least90%, preferably 95%, 98%, or more sequence identity to SEQ ID NO: 8.

In some embodiments, the amino acid substitution allows the addition ofheterologous molecules, e.g., PEG. In some embodiment, the a-HL varianthas post-translational modifications.

In some embodiments, the substitution is a non-native amino acid that isbasic or positively charged at a pH from about 5 to about 8.5.

In some instances, a polymerase is associated with the nanopore (e.g.,covalently linked to the nanopore) and the polymerase performsnucleotide incorporation events.

In an aspect, there is provided a heptomeric pore assembly comprising atleast one α-hemolysin (αHL) variant as described herein. In oneembodiment the invention provides a heteromeric pore assembly containinga mutant αHL polypeptide (M), e.g., a pore assembly which contains awild type (WT) staphylococcal αHL polypeptide and a mutant αHLpolypeptide in which an amino acid variant (as provided for herein) ofthe mutant αHL polypeptide occupies a position in a transmembranechannel of the pore structure. For example, the ratio of WT and variantαHL polypeptides is expressed by the formula WT_(7-n)M_(n), where n is1, 2, 3, 4, 5, 6, or 7; preferably the ratio of αHL polypeptides in theheteroheptamer is WT_(7-n)M_(n); most preferably, the ratio is WT₆M₁.Homomeric pores in which each subunit of the heptomer is a mutated αHLpolypeptide (i.e., where n=7) are also encompassed by the invention.

In an aspect, there is provided a nucleic acid encoding an a-HL variantas described herein.

In an aspect, there is provided a vector comprising a nucleic acidencoding an alpha-hemolysin variant as described herein.

In an aspect, there is provided a host cell transformed with the vectorcomprising a nucleic acid encoding an alpha-hemolysin variant asdescribed herein.

In an aspect, there is provided a method of producing an alpha-hemolysinvariant comprising the steps of: (a) culturing a host cell comprising anucleic acid encoding a alpha-hemolysin variant as described herein in asuitable culture medium under suitable conditions to producealpha-hemolysin variant; and (b) obtaining said produced alpha-hemolysinvariant.

In an aspect, there is provided a method for detecting a targetmolecule, comprising: (a) providing a chip comprising a nanopore asdescribed herein in a membrane that is disposed adjacent or in proximityto a sensing electrode; (b) directing a nucleic acid molecule throughsaid nanopore, wherein said nucleic acid molecule is associated with areporter molecule, wherein said nucleic acid molecule comprises anaddress region and a probe region, wherein said reporter molecule isassociated with said nucleic acid molecule at said probe region, andwherein said reporter molecule is coupled to a target molecule; (c)sequencing said address region while said nucleic acid molecule isdirected through said nanopore to determine a nucleic acid sequence ofsaid address region; and (d) identifying, with the aid of a computerprocessor, said target molecule based upon a nucleic acid sequence ofsaid address region determined in (c).

Other objects, features and advantages of the present invention willbecome apparent from the following detailed description. It should beunderstood, however, that the detailed description and specificexamples, while indicating preferred embodiments of the invention, aregiven by way of illustration only, since various changes andmodifications within the scope and spirit of the invention will becomeapparent to one skilled in the art from this detailed description.

BRIEF DESCRIPTION OF THE DRAWINGS

FIGS. 1-5 each comprise two figures, e.g., FIGS. 1A and 1B. The A figurefor each figure is a histogram of the number of capture events which hada “time-to-thread” equal to the time bin shown on the x-axis. The Bfigure for each figure is a portion of the raw data for thecorresponding figure A.

FIGS. 1A and 1B show the results for the wild-type a-hemolysin nanopore.FIG. 1A (top panel) shows “time-to-thread” data. This data is combinedfrom many pores which were capturing the tagged nucleotides indicatingthe pore had both a polymerase and a template DNA molecule. The mean andmedian values, along with the standard deviation for wild type aHL are20.7 ms, 16.1 ms and 1.5 ms respectively, and the total number ofsquarewaves used for the calculations is 41910.

FIG. 1B (bottom panel) shows some raw data with five consecutivesquarewaves shown. The data points between the green lines represent theopen channel (where no tagged nucleotide is threaded in the pore) andthe data in-between the red lines represents when the tagged nucleotidehas threaded into the pore and is blocking ions moving through thechannel. The electrode is cycled between positive and negative 100 mV,and in our system data points are not recorded when a negative voltageis applied. Thus, all the data points are collected from the positivelyapplied potential, and the time where there is an absence of data points(between 1716.9-1717 sec for example) is when the electrodes have anegative voltage applied to them. In this example the “time-to-thread”measurement is calculated from squarewaves which have a threaded levelobservable, and, the previous squarewave had a threaded level at the endof the positive voltage (indicating that the tag was threaded in thepore and bound by the polymerase).

FIGS. 2A and 2B show the results for the a-hemolysin nanopore comprisinga T12K mutation. FIG. 2A (top panel) is data combined from many poreswhich were capturing the tagged nucleotides indicating the pore had botha polymerase and a template DNA molecule. The mean and median values,along with the standard deviation for T12K aHL are 19.7 ms, 14.5 ms and1.5 ms respectively, and the total number of squarewaves used for thecalculations is 4311.

FIG. 2B (bottom panel) shows some raw data with five consecutivesquarewaves shown. The data points between the green lines represent theopen channel (where no tagged nucleotide is threaded in the pore) andthe data in-between the red lines represents when the tagged nucleotidehas threaded into the pore and is blocking ions moving through thechannel. The electrode is cycled between positive and negative 100 mV,and in our system data points are not recorded when a negative voltageis applied. Thus, all the data points are collected from the positivelyapplied potential, and the time where there is an absence of data points(between 1600.4-1601.2 sec for example) is when the electrodes have anegative voltage applied to them. In this example the “time-to-thread”measurement is calculated from squarewaves which have a threaded levelobservable, and, the previous squarewave had a threaded level at the endof the positive voltage (indicating that the tag was threaded in thepore and bound by the polymerase).

FIGS. 3A and 3B show the results for the a-hemolysin nanopore comprisinga T12R mutation. FIG. 3A is data combined from many pores which werecapturing the tagged nucleotides indicating the pore had both apolymerase and a template DNA molecule. The mean and median values,along with the standard deviation for T12R aHL are 16.9 ms, 10.5 ms and1.5 ms respectively, and the total number of squarewaves used for thecalculations is 4138.

FIG. 3B (bottom panel) shows some raw data with five consecutivesquarewaves shown. The data points between the green lines represent theopen channel (where no tagged nucleotide is threaded in the pore) andthe data in-between the red lines represents when the tagged nucleotidehas threaded into the pore and is blocking ions moving through thechannel. The electrode is cycled between positive and negative 100 mV,and in our system data points are not recorded when a negative voltageis applied. Thus, all the data points are collected from the positivelyapplied potential, and the time where there is an absence of data points(between 267.2-268.2 sec for example) is when the electrodes have anegative voltage applied to them. In this example the “time-to-thread”measurement is calculated from squarewaves which have a threaded levelobservable, and, the previous squarewave had a threaded level at the endof the positive voltage (indicating that the tag was threaded in thepore and bound by the polymerase).

FIGS. 4A and 4B show the results for the a-hemolysin nanopore comprisinga N17R mutation. FIG. 4A (top panel) is data combined from many poreswhich were capturing the tagged nucleotides indicating the pore had botha polymerase and a template DNA molecule. The mean and median values,along with the standard deviation for N17R aHL are 17.5 ms, 10.5 ms and1.7 ms respectively, and the total number of squarewaves used for thecalculations is 3877.

FIG. 4B (bottom panel) shows some raw data with five consecutivesquarewaves shown. The data points between the green lines represent theopen channel (where no tagged nucleotide is threaded in the pore) andthe data in-between the red lines represents when the tagged nucleotidehas threaded into the pore and is blocking ions moving through thechannel. The electrode is cycled between positive and negative 100 mV,and in our system data points are not recorded when a negative voltageis applied. Thus, all the data points are collected from the positivelyapplied potential, and the time where there is an absence of data points(between 344-344.9 sec for example) is when the electrodes have anegative voltage applied to them. In this example the “time-to-thread”measurement is calculated from squarewaves which have a threaded levelobservable, and, the previous squarewave had a threaded level at the endof the positive voltage (indicating that the tag was threaded in thepore and bound by the polymerase).

FIGS. 5A and 5B show the results for the a-hemolysin nanopore comprisinga N17K mutation. FIG. 5A (top panel) shows combined data from many poreswhich were capturing the tagged nucleotides indicating the pore had botha polymerase and a template DNA molecule. The mean and median values,along with the standard deviation for N17K aHL are 5.7 ms, 2.4 ms and0.7 ms respectively, and the total number of squarewaves used for thecalculations is 2424.

FIG. 5B (bottom panel) shows some raw data with five consecutivesquarewaves shown. The data points between the green lines represent theopen channel (where no tagged nucleotide is threaded in the pore) andthe data in-between the red lines represents when the tagged nucleotidehas threaded into the pore and is blocking ions moving through thechannel. The electrode is cycled between positive and negative 100 mV,and in our system data points are not recorded when a negative voltageis applied. Thus, all the data points are collected from the positivelyapplied potential, and the time where there is an absence of data points(between 79.5-80.5 sec for example) is when the electrodes have anegative voltage applied to them. In this example the “time-to-thread”measurement is calculated from squarewaves which have a threaded levelobservable, and, the previous squarewave had a threaded level at the endof the positive voltage (indicating that the tag was threaded in thepore and bound by the polymerase).

DETAILED DESCRIPTION

The invention will now be described in detail by way of reference onlyusing the following definitions and examples. All patents andpublications, including all sequences disclosed within such patents andpublications, referred to herein are expressly incorporated byreference.

Unless defined otherwise herein, all technical and scientific terms usedherein have the same meaning as commonly understood by one of ordinaryskill in the art to which this invention belongs. Singleton, et al.,DICTIONARY OF MICROBIOLOGY AND MOLECULAR BIOLOGY, 2D ED., John Wiley andSons, New York (1994), and Hale & Marham, THE HARPER COLLINS DICTIONARYOF BIOLOGY, Harper Perennial, NY (1991) provide one of skill with ageneral dictionary of many of the terms used in this invention. Althoughany methods and materials similar or equivalent to those describedherein can be used in the practice or testing of the present invention,the preferred methods and materials are described. Practitioners areparticularly directed to Sambrook et al., 1989, and Ausubel F M et al.,1993, for definitions and terms of the art. It is to be understood thatthis invention is not limited to the particular methodology, protocols,and reagents described, as these may vary.

Numeric ranges are inclusive of the numbers defining the range. The termabout is used herein to mean plus or minus ten percent (10%) of a value.For example, “about 100” refers to any number between 90 and 110.

Unless otherwise indicated, nucleic acids are written left to right in5′ to 3′ orientation; amino acid sequences are written left to right inamino to carboxy orientation, respectively.

The headings provided herein are not limitations of the various aspectsor embodiments of the invention which can be had by reference to thespecification as a whole. Accordingly, the terms defined immediatelybelow are more fully defined by reference to the specification as awhole.

Definitions

Alpha-hemolysin: As used herein, “alpha-hemolysin,” “α-hemolysin,”“a-HL” and “α-HL” are used interchangeably and refer to the monomericprotein that self-assembles into a heptameric water-filled transmembranechannel (i.e., nanopore). Depending on context, the term may also referto the transmembrane channel formed by seven monomeric proteins.

Amino acid: As used herein, the term “amino acid,” in its broadestsense, refers to any compound and/or substance that can be incorporatedinto a polypeptide chain. In some embodiments, an amino acid has thegeneral structure H₂N—C(H)(R)—COOH. In some embodiments, an amino acidis a naturally-occurring amino acid. In some embodiments, an amino acidis a synthetic amino acid; in some embodiments, an amino acid is aD-amino acid; in some embodiments, an amino acid is an L-amino acid.“Standard amino acid” refers to any of the twenty standard L-amino acidscommonly found in naturally occurring peptides. “Nonstandard amino acid”refers to any amino acid, other than the standard amino acids,regardless of whether it is prepared synthetically or obtained from anatural source. As used herein, “synthetic amino acid” or “non-naturalamino acid” encompasses chemically modified amino acids, including butnot limited to salts, amino acid derivatives (such as amides), and/orsubstitutions. Amino acids, including carboxy- and/or amino-terminalamino acids in peptides, can be modified by methylation, amidation,acetylation, and/or substitution with other chemical without adverselyaffecting their activity. Amino acids may participate in a disulfidebond. The term “amino acid” is used interchangeably with “amino acidresidue,” and may refer to a free amino acid and/or to an amino acidresidue of a peptide. It will be apparent from the context in which theterm is used whether it refers to a free amino acid or a residue of apeptide. It should be noted that all amino acid residue sequences arerepresented herein by formulae whose left and right orientation is inthe conventional direction of amino-terminus to carboxy-terminus.

Base Pair (bp): As used herein, base pair refers to a partnership ofadenine (A) with thymine (T), or of cytosine (C) with guanine (G) in adouble stranded DNA molecule.

Complementary: As used herein, the term “complementary” refers to thebroad concept of sequence complementarity between regions of twopolynucleotide strands or between two nucleotides through base-pairing.It is known that an adenine nucleotide is capable of forming specifichydrogen bonds (“base pairing”) with a nucleotide which is thymine oruracil. Similarly, it is known that a cytosine nucleotide is capable ofbase pairing with a guanine nucleotide.

Expression cassette: An “expression cassette” or “expression vector” isa nucleic acid construct generated recombinantly or synthetically, witha series of specified nucleic acid elements that permit transcription ofa particular nucleic acid in a target cell. The recombinant expressioncassette can be incorporated into a plasmid, chromosome, mitochondrialDNA, plastid DNA, virus, or nucleic acid fragment. Typically, therecombinant expression cassette portion of an expression vectorincludes, among other sequences, a nucleic acid sequence to betranscribed and a promoter.

Heterologous: A “heterologous” nucleic acid construct or sequence has aportion of the sequence which is not native to the cell in which it isexpressed. Heterologous, with respect to a control sequence refers to acontrol sequence (i.e. promoter or enhancer) that does not function innature to regulate the same gene the expression of which it is currentlyregulating. Generally, heterologous nucleic acid sequences are notendogenous to the cell or part of the genome in which they are present,and have been added to the cell, by infection, transfection,transformation, microinjection, electroporation, or the like. A“heterologous” nucleic acid construct may contain a control sequence/DNAcoding sequence combination that is the same as, or different from acontrol sequence/DNA coding sequence combination found in the nativecell.

Host cell: By the term “host cell” is meant a cell that contains avector and supports the replication, and/or transcription ortranscription and translation (expression) of the expression construct.Host cells for use in the present invention can be prokaryotic cells,such as E. coli or Bacillus subtilus, or eukaryotic cells such as yeast,plant, insect, amphibian, or mammalian cells. In general, host cells areprokaryotic, e.g., E. coli.

Isolated: An “isolated” molecule is a nucleic acid molecule that isseparated from at least one other molecule with which it is ordinarilyassociated, for example, in its natural environment. An isolated nucleicacid molecule includes a nucleic acid molecule contained in cells thatordinarily express the nucleic acid molecule, but the nucleic acidmolecule is present extrachromasomally or at a chromosomal location thatis different from its natural chromosomal location.

Modified alpha-hemolysin: As used herein, the term “modifiedalpha-hemolysin” refers to an alpha-hemolysin originated from another(i.e., parental) alpha-hemolysin and contains one or more amino acidalterations (e.g., amino acid substitution, deletion, or insertion)compared to the parental alpha-hemolysin. In some embodiments, amodified alpha-hemolysin of the invention is originated or modified froma naturally-occurring or wild-type alpha-hemolysin. In some embodiments,a modified alpha-hemolysin of the invention is originated or modifiedfrom a recombinant or engineered alpha-hemolysin including, but notlimited to, chimeric alpha-hemolysin, fusion alpha-hemolysin or anothermodified alpha-hemolysin. Typically, a modified alpha-hemolysin has atleast one changed phenotype compared to the parental alpha-hemolysin.

Mutation: As used herein, the term “mutation” refers to a changeintroduced into a parental sequence, including, but not limited to,substitutions, insertions, deletions (including truncations). Theconsequences of a mutation include, but are not limited to, the creationof a new character, property, function, phenotype or trait not found inthe protein encoded by the parental sequence.

Nanopore: The term “nanopore,” as used herein, generally refers to apore, channel or passage formed or otherwise provided in a membrane. Amembrane may be an organic membrane, such as a lipid bilayer, or asynthetic membrane, such as a membrane formed of a polymeric material.The membrane may be a polymeric material. The nanopore may be disposedadjacent or in proximity to a sensing circuit or an electrode coupled toa sensing circuit, such as, for example, a complementary metal-oxidesemiconductor (CMOS) or field effect transistor (FET) circuit. In someexamples, a nanopore has a characteristic width or diameter on the orderof 0.1 nanometers (nm) to about 1000 nm. Some nanopores are proteins.Alpha-hemolysin is an example of a protein nanopore.

Nucleic Acid Molecule: The term “nucleic acid molecule” includes RNA,DNA and cDNA molecules. It will be understood that, as a result of thedegeneracy of the genetic code, a multitude of nucleotide sequencesencoding a given protein such as alpha-hemolysin and/or variants thereofmay be produced. The present invention contemplates every possiblevariant nucleotide sequence, encoding variant alpha-hemolysin, all ofwhich are possible given the degeneracy of the genetic code.

Promoter: As used herein, the term “promoter” refers to a nucleic acidsequence that functions to direct transcription of a downstream gene.The promoter will generally be appropriate to the host cell in which thetarget gene is being expressed. The promoter together with othertranscriptional and translational regulatory nucleic acid sequences(also termed “control sequences”) are necessary to express a given gene.In general, the transcriptional and translational regulatory sequencesinclude, but are not limited to, promoter sequences, ribosomal bindingsites, transcriptional start and stop sequences, translational start andstop sequences, and enhancer or activator sequences.

Purified: As used herein, “purified” means that a molecule is present ina sample at a concentration of at least 95% by weight, or at least 98%by weight of the sample in which it is contained.

Purifying: As used herein, the term “purifying” generally refers tosubjecting transgenic nucleic acid or protein containing cells tobiochemical purification and/or column chromatography.

Tag: As used herein, the term “tag” refers to a detectable moiety thatmay be atoms or molecules, or a collection of atoms or molecules. A tagmay provide an optical, electrochemical, magnetic, or electrostatic(e.g., inductive, capacitive) signature, which signature may be detectedwith the aid of a nanopore. Typically, when a nucleotide is attached tothe tag it is called a “Tagged Nucleotide.” The tag may be attached tothe nucleotide via the phosphate moiety.

Time-To-Thread: The term “time to thread” or “TTT” means the time ittakes the polymerase-tag complex or a nucleic add strand to thread thetag into the barrel of the nanopore.

Variant: As used herein, the term “variant” refers to a modified proteinwhich displays altered characteristics when compared to the parentalprotein, e.g., altered ionic conductance.

Variant hemolysin: The term “variant hemolysin gene” or “varianthemolysin” means, respectively, that the nucleic acid sequence of thealpha-hemolysin gene from Staphylococcus aureus has been altered byremoving, adding, and/or manipulating the coding sequence or the aminoacid sequence of the expressed protein has been modified consistent withthe invention described herein.

Vector: As used herein, the term “vector” refers to a nucleic acidconstruct designed for transfer between different host cells. An“expression vector” refers to a vector that has the ability toincorporate and express heterologous DNA fragments in a foreign cell.Many prokaryotic and eukaryotic expression vectors are commerciallyavailable. Selection of appropriate expression vectors is within theknowledge of those having skill in the art.

Wild-type: As used herein, the term “wild-type” refers to a gene or geneproduct which has the characteristics of that gene or gene product whenisolated from a naturally-occurring source.

Percent homology: The term “% homology” is used interchangeably hereinwith the term “% identity” herein and refers to the level of nucleicacid or amino acid sequence identity between the nucleic acid sequencethat encodes any one of the inventive polypeptides or the inventivepolypeptide's amino acid sequence, when aligned using a sequencealignment program.

For example, as used herein, 80% homology means the same thing as 80%sequence identity determined by a defined algorithm, and accordingly ahomologue of a given sequence has greater than 80% sequence identityover a length of the given sequence. Exemplary levels of sequenceidentity include, but are not limited to, 80, 85, 90, 95, 98% or moresequence identity to a given sequence, e.g., the coding sequence for anyone of the inventive polypeptides, as described herein.

Exemplary computer programs which can be used to determine identitybetween two sequences include, but are not limited to, the suite ofBLAST programs, e.g., BLASTN, BLASTX, and TBLASTX, BLASTP and TBLASTN,publicly available on the Internet. See also, Altschul, et al., 1990 andAltschul, et al., 1997.

Sequence searches are typically carried out using the BLASTN programwhen evaluating a given nucleic acid sequence relative to nucleic acidsequences in the GenBank DNA Sequences and other public databases. TheBLASTX program is preferred for searching nucleic acid sequences thathave been translated in all reading frames against amino acid sequencesin the GenBank Protein Sequences and other public databases. Both BLASTNand BLASTX are run using default parameters of an open gap penalty of11.0, and an extended gap penalty of 1.0, and utilize the BLOSUM-62matrix. (See, e.g., Altschul, S. F., et al., Nucleic Acids Res.25:3389-3402, 1997.)

A preferred alignment of selected sequences in order to determine “%identity” between two or more sequences, is performed using for example,the CLUSTAL-W program in MacVector version 13.0.7, operated with defaultparameters, including an open gap penalty of 10.0, an extended gappenalty of 0.1, and a BLOSUM 30 similarity matrix.

Nomenclature

In the present description and claims, the conventional one-letter andthree-letter codes for amino acid residues are used.

For ease of reference, variants of the application are described by useof the following nomenclature:

Original amino acid(s): position(s): substituted amino acid(s).According to this nomenclature, for instance the substitution ofthreonine by an arginine in position 17 is shown as:

-   -   Thr17Arg or T17R

Multiple mutations are separated by plus signs, i.e.:

-   -   Thr17Arg+Glu34Ser or T17R+E345        representing mutations in positions 30 and 34 substituting        alanine and glutamic acid for asparagine and serine,        respectively.

When one or more alternative amino acid residues may be inserted in agiven position it is indicated as: T17R/K, or T17R or T17K.

Site-Directed Mutagenesis of Alpha-Hemolysin

Staphylococcus aureus alpha hemolysin wild type sequences are providedherein (SEQ ID NO:1, nucleic acid coding region; SEQ ID NO:3, proteincoding region) and available elsewhere (National Center forBioinformatics or GenBank Accession Numbers M90536 and AAA26598).

Point mutations may be introduced using QuikChange Lightning 2 kit(Stategene/Agilent) following manufacturer's instructions.

Primers can be ordered from commercial companies, e.g., IDT DNA.

Nanopore Assembly and Insertion

The methods described herein can use a nanopore having a polymeraseattached to the nanopore. In some cases, it is desirable to have one andonly one polymerase per nanopore (e.g., so that only one nucleic acidmolecule is sequenced at each nanopore). However, many nanopores,including alpha-hemolysin (aHL), can be multimeric proteins having aplurality of subunits (e.g., 7 subunits for aHL). The subunits can beidentical copies of the same polypeptide. Provided herein are multimericproteins (e.g., nanopores) having a defined ratio of modified subunits(e.g., a-HL variants) to un-modified subunits (e.g., a-HL). Alsoprovided herein are methods for producing multimeric proteins (e.g.,nanopores) having a defined ratio of modified subunits to un-modifiedsubunits.

With reference to FIG. 27 of WO2014/074727, a method for assembling aprotein having a plurality of subunits comprises providing a pluralityof first subunits 2705 and providing a plurality of second subunits2710, where the second subunits are modified when compared with thefirst subunits. In some cases, the first subunits are wild-type (e.g.,purified from native sources or produced recombinantly). The secondsubunits can be modified in any suitable way. In some cases, the secondsubunits have a protein (e.g., a polymerase) attached (e.g., as a fusionprotein).

The modified subunits can comprise a chemically reactive moiety (e.g.,an azide or an alkyne group suitable for forming a linkage). In somecases, the method further comprises performing a reaction (e.g., a Clickchemistry cycloaddition) to attach an entity (e.g., a polymerase) to thechemically reactive moiety.

The method can further comprise contacting the first subunits with thesecond subunits 2715 in a first ratio to form a plurality of proteins2720 having the first subunits and the second subunits. For example, onepart modified aHL subunits having a reactive group suitable forattaching a polymerase can be mixed with six parts wild-type aHLsubunits (i.e., with the first ratio being 1:6). The plurality ofproteins can have a plurality of ratios of the first subunits to thesecond subunits. For example, the mixed subunits can form severalnanopores having a distribution of stoichiometries of modified toun-modified subunits (e.g., 1:6, 2:5, 3:4).

In some cases, the proteins are formed by simply mixing the subunits. Inthe case of aHL nanopores for example, a detergent (e.g., deoxycholicacid) can trigger the aHL monomer to adopt the pore conformation. Thenanopores can also be formed using a lipid (e.g.,1,2-diphytanoyl-sn-glycero-3-phosphocholine (DPhPC) or1,2-di-0-phytanyl-sn-glycero-3-phosphocholine (DoPhPC)) and moderatetemperature (e.g., less than about 100° C.). In some cases, mixing DPhPCwith a buffer solution creates large multi-lamellar vesicles (LMV), andadding aHL subunits to this solution and incubating the mixture at 40°C. for 30 minutes results in pore formation.

If two different types of subunits are used (e.g., the natural wild typeprotein and a second aHL monomer which can contain a single pointmutation), the resulting proteins can have a mixed stoichiometry (e.g.,of the wild type and mutant proteins). The stoichiometry of theseproteins can follow a formula which is dependent upon the ratio of theconcentrations of the two proteins used in the pore forming reaction.This formula is as follows:100P _(m)=100[n!m!(n−m)!]·f _(mut) ^(m) ·f _(wt) ^(n˜m), where

-   -   P_(m)=probability of a pore having m number of mutant subunits    -   n=total number of subunits (e.g., 7 for aHL)    -   m=number of “mutant” subunits    -   f_(mut)=fraction or ratio of mutant subunits mixed together    -   f_(wt)=fraction or ratio of wild-type subunits mixed together

The method can further comprise fractionating the plurality of proteinsto enrich proteins that have a second ratio of the first subunits to thesecond subunits 2725. For example, nanopore proteins can be isolatedthat have one and only one modified subunit (e.g., a second ratio of1:6). However, any second ratio is suitable. A distribution of secondratios can also be fractionated such as enriching proteins that haveeither one or two modified subunits. The total number of subunitsforming the protein is not always 7 (e.g., a different nanopore can beused or an alpha-hemolysin nanopore can form having six subunits) asdepicted in FIG. 27 of WO2014/074727. In some cases, proteins havingonly one modified subunit are enriched. In such cases, the second ratiois 1 second subunit per (n−1) first subunits where n is the number ofsubunits comprising the protein.

The first ratio can be the same as the second ratio, however this is notrequired. In some cases, proteins having mutated monomers can form lessefficiently than those not having mutated subunits. If this is the case,the first ratio can be greater than the second ratio (e.g., if a secondratio of 1 mutated to 6 non-mutated subunits are desired in a nanopore,forming a suitable number of 1:6 proteins may require mixing thesubunits at a ratio greater than 1:6).

Proteins having different second ratios of subunits can behavedifferently (e.g., have different retention times) in a separation. Insome cases, the proteins are fractionated using chromatography, such asion exchange chromatography or affinity chromatography. Since the firstand second subunits can be identical apart from the modification, thenumber of modifications on the protein can serve as a basis forseparation. In some cases, either the first or second subunits have apurification tag (e.g., in addition to the modification) to allow orimprove the efficiency of the fractionation. In some cases, apoly-histidine tag (His-tag), a streptavidin tag (Strep-tag), or otherpeptide tag is used. In some instances, the first and second subunitseach comprise different tags and the fractionation step fractionates onthe basis of each tag. In the case of a His-tag, a charge is created onthe tag at low pH (Histidine residues become positively charged belowthe pKa of the side chain). With a significant difference in charge onone of the aHL molecules compared to the others, ion exchangechromatography can be used to separate the oligomers which have 0, 1, 2,3, 4, 5, 6, or 7 of the “charge-tagged” aHL subunits. In principle, thischarge tag can be a string of any amino acids which carry a uniformcharge. FIG. 28 and FIG. 29 show examples of fractionation of nanoporesbased on a His-tag. FIG. 28 shows a plot of ultraviolet absorbance at280 nanometers, ultraviolet absorbance at 260 nanometers, andconductivity. The peaks correspond to nanopores with various ratios ofmodified and unmodified subunits. FIG. 29 of WO2014/074727 showsfractionation of aHL nanopores and mutants thereof using both His-tagand Strep-tags.

In some cases, an entity (e.g., a polymerase) is attached to the proteinfollowing fractionation. The protein can be a nanopore and the entitycan be a polymerase. In some instances, the method further comprisesinserting the proteins having the second ratio subunits into a bilayer.

In some situations, a nanopore can comprise a plurality of subunits. Apolymerase can be attached to one of the subunits and at least one andless than all of the subunits comprise a first purification tag. In someexamples, the nanopore is alpha-hemolysin or a variant thereof. In someinstances, all of the subunits comprise a first purification tag or asecond purification tag. The first purification tag can be apoly-histidine tag (e.g., on the subunit having the polymeraseattached).

Polymerase Attached to Nanopore

In some cases, a polymerase (e.g., DNA polymerase) is attached to and/oris located in proximity to the nanopore. The polymerase can be attachedto the nanopore before or after the nanopore is incorporated into themembrane. In some instances, the nanopore and polymerase are a fusionprotein (i.e., single polypeptide chain).

The polymerase can be attached to the nanopore in any suitable way. Insome cases, the polymerase is attached to the nanopore (e.g., hemolysin)protein monomer and then the full nanopore heptamer is assembled (e.g.,in a ratio of one monomer with an attached polymerase to 6 nanopore(e.g., hemolysin) monomers without an attached polymerase). The nanoporeheptamer can then be inserted into the membrane.

Another method for attaching a polymerase to a nanopore involvesattaching a linker molecule to a hemolysin monomer or mutating ahemolysin monomer to have an attachment site and then assembling thefull nanopore heptamer (e.g., at a ratio of one monomer with linkerand/or attachment site to 6 hemolysin monomers with no linker and/orattachment site). A polymerase can then be attached to the attachmentsite or attachment linker (e.g., in bulk, before inserting into themembrane). The polymerase can also be attached to the attachment site orattachment linker after the (e.g., heptamer) nanopore is formed in themembrane. In some cases, a plurality of nanopore-polymerase pairs areinserted into a plurality of membranes (e.g., disposed over the wellsand/or electrodes) of the biochip. In some instances, the attachment ofthe polymerase to the nanopore complex occurs on the biochip above eachelectrode.

The polymerase can be attached to the nanopore with any suitablechemistry (e.g., covalent bond and/or linker). In some cases, thepolymerase is attached to the nanopore with molecular staples. In someinstances, molecular staples comprise three amino acid sequences(denoted linkers A, B and C). Linker A can extend from a hemolysinmonomer, Linker B can extend from the polymerase, and Linker C then canbind Linkers A and B (e.g., by wrapping around both Linkers A and B) andthus the polymerase to the nanopore. Linker C can also be constructed tobe part of Linker A or Linker B, thus reducing the number of linkermolecules.

In some instances, the polymerase is linked to the nanopore usingSolulink™ chemistry. Solulink™ can be a reaction between HyNic(6-hydrazino-nicotinic acid, an aromatic hydrazine) and 4FB(4-formylbenzoate, an aromatic aldehyde). In some instances, thepolymerase is linked to the nanopore using Click chemistry (availablefrom LifeTechnologies for example). In some cases, zinc finger mutationsare introduced into the hemolysin molecule and then a molecule is used(e.g., a DNA intermediate molecule) to link the polymerase to the zincfinger sites on the hemolysin.

Apparatus Set-Up

The nanopore may be formed or otherwise embedded in a membrane disposedadjacent to a sensing electrode of a sensing circuit, such as anintegrated circuit. The integrated circuit may be an applicationspecific integrated circuit (ASIC). In some examples, the integratedcircuit is a field effect transistor or a complementary metal-oxidesemiconductor (CMOS). The sensing circuit may be situated in a chip orother device having the nanopore, or off of the chip or device, such asin an off-chip configuration. The semiconductor can be anysemiconductor, including, without limitation, Group IV (e.g., silicon)and Group III-V semiconductors (e.g., gallium arsenide). See, forexample, WO 2013/123450, for the apparatus and device set-up for sensinga nucleotide or tag.

Pore based sensors (e.g., biochips) can be used forelectro-interrogation of single molecules. A pore based sensor caninclude a nanopore of the present disclosure formed in a membrane thatis disposed adjacent or in proximity to a sensing electrode. The sensorcan include a counter electrode. The membrane includes a trans side(i.e., side facing the sensing electrode) and a cis side (i.e., sidefacing the counter electrode).

In the experimental disclosure which follows, the followingabbreviations apply: eq (equivalents); M (Molar); μM (micromolar); N(Normal); mol (moles); mmol (millimoles); μmol (micromoles); nmol(nanomoles); g (grams); mg (milligrams); kg (kilograms); μg(micrograms); L (liters); ml (milliliters); μl (microliters); cm(centimeters); mm (millimeters); μm (micrometers); nm (nanometers); ° C.(degrees Centigrade); h (hours); min (minutes); sec (seconds); msec(milliseconds).

EXAMPLES

The present invention is described in further detain in the followingexamples which are not in any way intended to limit the scope of theinvention as claimed. The attached Figures are meant to be considered asintegral parts of the specification and description of the invention.All references cited are herein specifically incorporated by referencefor all that is described therein. The following examples are offered toillustrate, but not to limit the claimed invention.

Example 1 Expression and Recovery

This example illustrates the expression and recovery of protein frombacterial host cells, e.g., E. coli.

DNA encoding the wild-type a-HL was purchased from a commercial source.The sequence was verified by sequencing.

Plasmid Construction.

The gene encoding either a wild-type or variant α-hemolysin was insertedinto a pPR-IBA2 plasmid (IBA Life Sciences, Germany) under the controlof T7 promoter.

Transformation.

E. coli BL21 DE3 (from Life Technologies) cells were transformed withthe expression vector comprising the DNA encoding the wild-type orvariant α-hemolysin using techniques well-known in the art. Briefly, thecells were thawed on ice (if frozen). Next, the desired DNA (in asuitable vector/plasmid) was added directly into the competent cells(should not exceed 5% of that of the competent cells) and mixed byflicking the tube. The tubes were placed on ice for 20 minutes. Next,the cells were placed in a 42° C. water bath for 45 seconds withoutmixing, followed by placing the tubes on ice for 2 min. The cells werethen transferred to a 15 ml sterilized culture tube containing 0.9 ml ofSOC medium (pre-warmed at room temperature) and cultured at 37° C. for 1hr in a shaker. Finally, an aliquot of the cells were spread onto a LBagar plate containing the appropriate antibiotic and the platesincubated at 37° C. overnight.

Protein Expression.

Following transformation, colonies were picked and inoculated into asmall volume (e.g., 3 ml) of growth medium (e.g., LB broth) containingthe appropriate antibiotic with shaking at 37° C., overnight.

The next morning, transfer 1 ml of the overnight culture to a new 100 mlof autoinduction medium, e.g., Magic Media (Life Technologies)containing an appropriate antibiotic to select the expression plasmid.Grow the culture with shaking at 25° C. approximately 16 hrs but thisdepended on the expression plasmids. Cells were harvested bycentrifugation at 3,000 g for 20 min at 4° C. and stored at −80° C.until used.

Purification.

Cells were lysed via sonication. The alpha-hemolysin was purified tohomogeneity by affinity column chromatography.

Example 2 T12 and/or N17 Variants

The following example details the introduction of a mutation at adesired residue.

Mutations.

Site-directed mutagenesis is carried out using a QuikChange MultiSite-Directed Mutagenesis kit (Stratagene, La Jolla, Calif.) to preparethe T12 and/or N17 variants.

The variants were expressed and purified as in Example 1.

Example 3 Assembly of Nanopore

This example describes the assembly of a nanopore comprising six a-HLvariant subunits and one wild-type subunit.

The wild-type a-HL was expressed as described in Example 1 with SpyTagand a HisTag and purified on a cobalt affinity column using a cobaltelution buffer (200 mM NaCl, 300 mM imidazole, 50 mM tris, pH 8). Thedesired a-HL variant was expressed as described in Example 1 with aStrepTag and purified using a Streptactin affinity column on the fastprotein liquid chromatography (FPLC) using an elution buffer (50 mMtris, 5 mM desthiobiotin, 200 mM NaCl, pH 8). The proteins were storedat 4° C. if used within 5 days, otherwise 8% trehalose was added andstored at −80° C.

Using approximately 20 mg of total protein, the wild-type a-HL todesired a-HL variant solutions were mixed together at the 1:6 ratio.Diphytanoylphosphatidylcholine (DPhPC) lipid was solubilized in either50 mM Tris, 200 mM NaCl, pH 8 or 150 mM KCl, 30 mM HEPES, pH 7.5 to afinal concentration of 50 mg/ml and added to the mixture of a-HLmonomers to a final concentration of 5 mg/ml. The mixture of the a-HLmonomers was incubated at 40° C. for at least 10 min. The lipidhemolysin mixture is applied to a size-exclusion chromatography columnto separate the lipid from the oligomerized proteins.

Example 4 Attachment of a Polymerase

This example provides for the attachment of a polymerase to a nanopore.

The polymerase may be coupled to the nanopore by any suitable means.See, for example, PCT/US2013/068967 (published as WO2014/074727; GeniaTechnologies), PCT/US2005/009702 (published as WO2006/028508), andPCT/US2011/065640 (published as WO2012/083249; Columbia Univ).

The polymerase, e.g., phi29 DNA Polymerase, was coupled to a proteinnanopore (e.g. alpha-hemolysin), through a linker molecule.Specifically, the SpyTag and SpyCatcher system, that spontaneously formscovalent isopeptide linkages under physiological conditions was used.See, for example, Li et al, J Mol Biol. 2014 Jan. 23; 426(2):309-17.

The Sticky phi29 SpyCatcher HisTag was expressed according to Example 1and purified using a cobalt affinity column. The SpyCatcher polymeraseand the SpyTag oligomerized protein were incubated overnight at 4° C. in3 mM SrCl₂. The 1:6-polymerase-template complex is then purified usingsize-exclusion chromatography.

Example 5 Activity of the Variants

This example shows the activity of the nanopores as provided by Example3 (nanopores with an attached polymerase).

The wild-type and variant nonpores were assayed to determine the effectof a mutation at one or more positions. The assay was designed tomeasure the time it takes to capture a tagged molecule by a DNApolymerase attached to the nanopore using alternating voltages, i.e.,squarewaves.

The bilayers were formed and pores were inserted as described inPCT/US14/61853 filed 23 Oct. 2014. The nanopore device (or sensor) usedto detect a molecule (and/or sequence a nucleic acid) was set-up asdescribed in WO2013123450.

To measure the time it takes to capture a tagged nucleotide by a DNApolymerase in our sequencing complex we have devised an assay that usesalternating positive and negative voltages (squarewaves) to determinethe amount of time this takes. Our sequencing complex is comprised of aprotein nanopore (αHL) which is attached to a single DNA polymerase (seeExample 4). The tagged nucleotides are negatively charged, and aretherefore attracted to the nanopore when the voltage applied is positivein nature, and repelled when the voltage applied to the nanoporesequencing complex is negative. So we can measure the time it takes fora tag to thread into the pore by cycling the voltage between positiveand negative potentials and determine how much time the nanopore'scurrent is unobstructed (open channel) verses when the tag is threaded(reduced current flux).

To carry out this “time-to-thread” assay the Genia Sequencing device isused with a Genia Sequencing Chip. The electrodes are conditioned andphospholipid bilayers are established on the chip as explained inPCT/US2013/026514. Genia's sequencing complex is inserted to thebilayers following the protocol described in PCT/US2013/026514(published as WO2013/123450). The time-to-thread data shown in thispatent was collected using a buffer system comprised of 20 mM HEPES pH7.5, 300 mM KCl, 3 uM tagged nucleotide, 3 mM Ca²⁺, with a voltageapplied of +/−100 mV with a duty cycle of 5 Hz. After the data wascollected it was analyzed for squarewaves that showed the capture of atagged nucleotide (threaded level) which lasted to the end of thepositive portion of the squarewave, and was followed by another tagcapture on the subsequent squarewave. The time-to-thread was measured bydetermining how long the second squarewave reported unobstructed openchannel current. As an example, if 10 consecutive squarewaves showedtagged nucleotide captures that lasted to the end of the positiveportion of the squarewave then the time-to-thread parameter would becalculated from squarewaves 2-10 (the first squarewave does not factorinto the calculation because the polymerase did not have a tag bound toit in the previous squarewave). These time-to-thread numbers were thencollected for all of the pores in the experiment and statisticalparameters extracted from them (such as a mean, median, standarddeviation etc.).

Results are shown in FIGS. 1-5.

It is understood that the examples and embodiments described herein arefor illustrative purposes only and that various modifications or changesin light thereof will be suggested to persons skilled in the art and areto be included within the spirit and purview of this application andscope of the appended claims. All publications, patents, and patentapplications cited herein are hereby incorporated by reference in theirentirety for all purposes.

SEQUENCE LISTING FREE TEXT SEQ ID NO: 1 (WT aHL DNA)ATGGCAGATC TCGATCCCGC GAAATTAATA CGACTCACTA TAGGGAGGCC 50ACAACGGTTT CCCTCTAGAA ATAATTTTGT TTAACTTTAA GAAGGAGATA 100TACAAATGGA TTCAGATATT AATATTAAAA CAGGTACAAC AGATATTGGT 150TCAAATACAA CAGTAAAAAC TGGTGATTTA GTAACTTATG ATAAAGAAAA 200TGGTATGCAT AAAAAAGTAT TTTATTCTTT TATTGATGAT AAAAATCATA 250ATAAAAAATT GTTAGTTATT CGTACAAAAG GTACTATTGC AGGTCAATAT 300AGAGTATATA GTGAAGAAGG TGCTAATAAA AGTGGTTTAG CATGGCCATC 350TGCTTTTAAA GTTCAATTAC AATTACCTGA TAATGAAGTA GCACAAATTT 400CAGATTATTA TCCACGTAAT AGTATTGATA CAAAAGAATA TATGTCAACA 450TTAACTTATG GTTTTAATGG TAATGTAACA GGTGATGATA CTGGTAAAAT 500TGGTGGTTTA ATTGGTGCTA ATGTTTCAAT TGGTCATACA TTAAAATATG 550TACAACCAGA TTTTAAAACA ATTTTAGAAA GTCCTACTGA TAAAAAAGTT 600GGTTGGAAAG TAATTTTTAA TAATATGGTT AATCAAAATT GGGGTCCTTA 650TGATCGTGAT AGTTGGAATC CTGTATATGG TAATCAATTA TTTATGAAAA 700CAAGAAATGG TTCTATGAAA GCAGCTGATA ATTTCTTAGA TCCAAATAAA 750GCATCAAGTT TATTATCTTC AGGTTTTTCT CCTGATTTTG CAACAGTTAT 800TACTATGGAT AGAAAAGCAT CAAAACAACA AACAAATATT GATGTTATTT 850ATGAACGTGT AAGAGATGAT TATCAATTAC ATTGGACATC AACTAATTGG 900AAAGGTACAA ATACTAAAGA TAAATGGACA GATAGAAGTT CAGAAAGATA 950TAAAATTGAT TGGGAAAAAG AAGAAATGAC AAATGGTCTC AGCGCTTGGA 1000GCCACCCGCA GTTCGAAAAA TAA 1023SEQ ID NO: 2 (WT aHL amino acids)[as expressed in E. coli]MADSDINIKT GTTDIGSNTT VKTGDLVTYD KENGMHKKVF YSFIDDKNHN 50KKLLVIRTKG TIAGQYRVYS EEGANKSGLA WPSAFKVQLQ LPDNEVAQIS 100DYYPRNSIDT KEYMSTLTYG FNGNVTGDDT GKIGGLIGAN VSIGHTLKYV 150QPDFKTILES PTDKKVGWKV IFNNMVNQNW GPYDRDSWNP VYGNQLFMKT 200RNGSMKAADN FLDPNKASSL LSSGFSPDFA TVITMDRKAS KQQTNIDVIY 250ERVRDDYQLH WTSTNWKGTN TKDKWTDRSS ERYKIDWEKE EMTNGLSAWS 300 HPQFEK 306SEQ ID NO: 3 (Mature WT aHL sequence for numbering)ADSDINIKTG TTDIGSNTTV KTGDLVTYDK ENGMHKKVFY SFIDDKNHNK 50KLLVIRTKGT IAGQYRVYSE EGANKSGLAW PSAFKVQLQL PDNEVAQISD 100YYPRNSIDTK EYMSTLTYGF NGNVTGDDTG KIGGLIGANV SIGHTLKYVQ 150PDFKTILESP TDKKVGWKVI FNNMVNQNWG PYDRDSWNPV YGNQLFMKTR 200NGSMKAADNF LDPNKASSLL SSGFSPDFAT VITMDRKASK QQTNIDVIYE 250RVRDDYQLHW TSTNWKGTNT KDKWTDRSSE RYKIDWEKEE MTNGLSAWSH 300 PQFEK 305SEQ ID NO: 4 (N17K aHL amino acids) ADSDINIKTG TTDIGS KTTV KTGDLVTYDK ENGMHKKVFY SFIDDKNHNK 50KLLVIRTKGT IAGQYRVYSE EGANKSGLAW PSAFKVQLQL PDNEVAQISD 100YYPRNSIDTK EYMSTLTYGF NGNVTGDDTG KIGGLIGANV SIGHTLKYVQ 150PDFKTILESP TDKKVGWKVI FNNMVNQNWG PYDRDSWNPV YGNQLFMKTR 200NGSMKAADNF LDPNKASSLL SSGFSPDFAT VITMDRKASK QQTNIDVIYE 250RVRDDYQLHW TSTNWKGTNT KDKWTDRSSE RYKIDWEKEE MTNGLSAWSH 300 PQFEK 305SEQ ID NO: 5 (N17R aHL amino acids) ADSDINIKTG TTDIGS RTTV KTGDLVTYDK ENGMHKKVFY SFIDDKNHNK 50KLLVIRTKGT IAGQYRVYSE EGANKSGLAW PSAFKVQLQL PDNEVAQISD 100YYPRNSIDTK EYMSTLTYGF NGNVTGDDTG KIGGLIGANV SIGHTLKYVQ 150PDFKTILESP TDKKVGWKVI FNNMVNQNWG PYDRDSWNPV YGNQLFMKTR 200NGSMKAADNF LDPNKASSLL SSGFSPDFAT VITMDRKASK QQTNIDVIYE 250RVRDDYQLHW TSTNWKGTNT KDKWTDRSSE RYKIDWEKEE MTNGLSAWSH 300 PQFEK 305SEQ ID NO: 6 (T12K aHL amino acids) ADSDINIKTG T KDIGSNTTV KTGDLVTYDK ENGMHKKVFY SFIDDKNHNK 50KLLVIRTKGT IAGQYRVYSE EGANKSGLAW PSAFKVQLQL PDNEVAQISD 100YYPRNSIDTK EYMSTLTYGF NGNVTGDDTG KIGGLIGANV SIGHTLKYVQ 150PDFKTILESP TDKKVGWKVI FNNMVNQNWG PYDRDSWNPV YGNQLFMKTR 200NGSMKAADNF LDPNKASSLL SSGFSPDFAT VITMDRKASK QQTNIDVIYE 250RVRDDYQLHW TSTNWKGTNT KDKWTDRSSE RYKIDWEKEE MTNGLSAWSH 300 PQFEK 305SEQ ID NO: 7 (T12R aHL amino acids) ADSDINIKTG T RDIGSNTTV KTGDLVTYDK ENGMHKKVFY SFIDDKNHNK 50KLLVIRTKGT IAGQYRVYSE EGANKSGLAW PSAFKVQLQL PDNEVAQISD 100YYPRNSIDTK EYMSTLTYGF NGNVTGDDTG KIGGLIGANV SIGHTLKYVQ 150PDFKTILESP TDKKVGWKVI FNNMVNQNWG PYDRDSWNPV YGNQLFMKTR 200NGSMKAADNF LDPNKASSLL SSGFSPDFAT VITMDRKASK QQTNIDVIYE 250RVRDDYQLHW TSTNWKGTNT KDKWTDRSSE RYKIDWEKEE MTNGLSAWSH 300 PQFEK 305SEQ ID NO: 8 (Mature WT aHL; AAA26598)ADSDINIKTG TTDIGSNTTV KTGDLVTYDK ENGMHKKVFY SFIDDKNHNK 50KLLVIRTKGT IAGQYRVYSE EGANKSGLAW PSAFKVQLQL PDNEVAQISD 100YYPRNSIDTK EYMSTLTYGF NGNVTGDDTG KIGGLIGANV SIGHTLKYVQ 150PDFKTILESP TDKKVGWKVI FNNMVNQNWG PYDRDSWNPV YGNQLFMKTR 200NGSMKAADNF LDPNKASSLL SSGFSPDFAT VITMDRKASK QQTNIDVIYE 250RVRDDYQLHW TSTNWKGTNT KDKWTDRSSE RYKIDWEKEE MTN 293

CITATION LIST Patent Literature

-   [1] PCT/US2013/026514 (published as WO2013/123450) entitled “Methods    for Creating Bilayers for Use with Nanopore Sensors”-   [2] PCT/US2013/068967 (published as WO 2014/074727) entitled    “Nucleic Acid Sequencing Using Tags”-   [3] PCT/US14/61853 filed 23 Oct. 2014 entitled “Methods for Forming    Lipid Bilayers on Biochips”

Non-Patent Literature

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The entirety of each patent, patent application, publication, document,GENBANK sequence, website and other published material referenced hereinhereby is incorporated by reference, including all tables, drawings, andfigures. All patents and publications are herein incorporated byreference to the same extent as if each was specifically andindividually indicated to be incorporated by reference. Citation of theabove patents, patent applications, publications and documents is not anadmission that any of the foregoing is pertinent prior art, nor does itconstitute any admission as to the contents or date of thesepublications or documents. All patents and publications mentioned hereinare indicative of the skill levels of those of ordinary skill in the artto which the invention pertains.

What is claimed is:
 1. An α-hemolysin (α-HL) variant comprising asubstitution at a position corresponding to position 17 of SEQ ID NO:3,wherein the substitution is a positive charge substitution.
 2. Theα-hemolysin variant according to claim 1, wherein said variant furthercomprises H144A.
 3. The α-hemolysin variant according to claim 1 or 2,wherein said variant comprises a substitution at positions correspondingto residue N17.
 4. The α-hemolysin variant according to claim 1 or 2,wherein said variant comprises a substitution selected from N17K, N17Rand combinations thereof.
 5. The α-hemolysin (α-HL) variant according toclaim 1, wherein the substitution is N17K.
 6. The α-hemolysin (α-HL)variant according to claim 1, wherein the substitution is N17R.
 7. Theα-hemolysin (α-HL) variant according to claim 1, wherein the variant hasa sequence having at least 80%, 90%, 95%, 98%, or more sequence identityto SEQ ID NO:
 8. 8. An alpha-hemolysin variant according to claim 1 or2, which is covalently bound to a DNA polymerase.
 9. An alpha-hemolysinvariant according to claim 8, wherein said variant is bound to the DNApolymerase via an isopeptide bond.
 10. A heptameric nanopore assemblycomprising at least one α-hemolysin (α-HL) variant according to any oneof claim 1 or
 2. 11. The heptameric nanopore assembly according to claim10, wherein said pore assembly has an altered time to thread (TTT)relative to a pore complex consisting of native alpha-hemolysin.
 12. Theheptameric nanopore assembly according to claim 11, wherein the TTT isdecreased.
 13. A method for detecting a target molecule, comprising: (a)providing a chip comprising a nanopore according to claim 10 in amembrane that is disposed adjacent or in proximity to a sensingelectrode; (b) directing a nucleic acid molecule through said nanopore,wherein said nucleic acid molecule is associated with a reportermolecule, wherein said nucleic acid molecule comprises an address regionand a probe region, wherein said reporter molecule is associated withsaid nucleic acid molecule at said probe region, and wherein saidreporter molecule is coupled to a target molecule; (c) sequencing saidaddress region while said nucleic acid molecule is directed through saidnanopore to determine a nucleic acid sequence of said address region;and (d) identifying, with the aid of a computer processor, said targetmolecule based upon a nucleic acid sequence of said address regiondetermined in (c).